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Soligenix Inc. Reports Promising Interim Results for HyBryte(TM) in Early-Stage Cutaneous T-Cell Lymphoma Treatment

By Advos

TL;DR

Soligenix's HyBryte(TM) offers a competitive edge in treating early-stage CTCL, presenting a novel option in a market with limited FDA-approved therapies.

HyBryte(TM) therapy, administered twice weekly for up to 54 weeks, shows promising results in early-stage CTCL treatment, as per interim IIS data.

HyBryte(TM) by Soligenix improves CTCL patients' lives, offering hope and a safer alternative in a field lacking new treatments for over a decade.

Discover how Soligenix's HyBryte(TM) is changing CTCL treatment landscapes with its innovative approach and promising early-stage results.

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Soligenix Inc. Reports Promising Interim Results for HyBryte(TM) in Early-Stage Cutaneous T-Cell Lymphoma Treatment

Soligenix Inc. (NASDAQ: SNGX) has announced encouraging interim results from its ongoing investigator-initiated study of HyBryte(TM), a potential treatment for early-stage cutaneous T-cell lymphoma (CTCL). The study, led by Ellen Kim, MD, director of the Penn Cutaneous Lymphoma Program, indicates promising success rates for patients with limited treatment options. With no new FDA-approved, skin-directed therapies introduced in over a decade, HyBryte(TM) represents a significant advancement in the field.

The interim results from the open-label study, which evaluates extended HyBryte(TM) therapy administered twice weekly for up to 54 weeks, showed positive outcomes at the 18-week evaluation point. This development is particularly noteworthy given the risks associated with conventional treatment options for CTCL patients. The study's findings, shared in collaboration with the Cutaneous Lymphoma Foundation, highlight the potential of HyBryte(TM) to fill a critical gap in CTCL treatment.

For more detailed information on the study and its implications, visit https://ibn.fm/IUoEe. Investors and interested parties can find the latest updates on Soligenix Inc. at https://ibn.fm/SNGX.

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Advos

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